| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:5097728-5098030 | Common:4; Rare:104 | ||||
| chr16:8621573-8621762 | Common:1; Rare:72 | ||||
| chr16:8674319-8674655 | Common:2; Rare:113; Clinvar:2 | ||||
| chr16:8797621-8797866 | Rare:93; Clinvar:2; Clinvar (benign):1 | ||||
| chr16:8868977-8869251 | Common:4; Rare:122 | ||||
| chr16:10580581-10580642 | Rare:19 | ||||
| chr16:10580649-10580843 | Common:2; Rare:70 | ||||
| chr16:10944332-10944591 | Common:1; Rare:75 | ||||
| chr16:11345216-11345457 | Common:1; Rare:74 | ||||
| chr16:11851489-11851645 | Common:1; Rare:79 | ||||
| chr16:11915397-11915709 | Common:5; Rare:113 | ||||
| chr16:11915897-11916215 | Common:2; Rare:128 | ||||
| chr16:11976615-11976734 | Common:2; Rare:42 | ||||
| chr16:14071034-14071365 | Common:4; Rare:116 | ||||
| chr16:14630170-14630484 | Rare:122 |